Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/86031
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dc.contributor.authorWarrener, R.-
dc.contributor.authorHarrison, P.-
dc.contributor.authorSterns, M.-
dc.contributor.authorRussell, R.-
dc.date.issued1984-
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1984; 1984(8):546-548-
dc.identifier.issn0022-4936-
dc.identifier.urihttp://hdl.handle.net/2440/86031-
dc.description.abstractCyclobutano[a]indene is characterised for the first time and shown to undergo a selection of cycloaddition reactions, including self-dimerisation to a [π2 +π2] dimmer whose structure has been confirmed by single crystal X-ray analysis.-
dc.description.statementofresponsibilityRonald N. Warrener, Peter A. Harrison, Meta Sterns and Richard A. Russell-
dc.language.isoen-
dc.publisherRoyal Society of Chemistry-
dc.rightsCopyright status unknown-
dc.titleCyclobutano[a]indene: a highly reactive strained olefin which plays a key trapping role in the photodecomposition of a polycyclic α-dione-
dc.title.alternativeCyclobutano[a]indene: a highly reactive strained olefin which plays a key trapping role in the photodecomposition of a polycyclic alpha-dione-
dc.typeJournal article-
dc.identifier.doi10.1039/c39840000546-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 7
Chemistry publications

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